Web sites:
The Centre for Applied Genomics
The Chromosome 7 Project
Database of Genomic Variants

News:
Press Releases and Articles
Lay Reviews/Opinions/Editorials
Media/Scientific News Articles
Interviews
Video presentation and interview
Integrative research at TCAG [Video]

Contact Info:
Stephen W. Scherer
The Centre for Applied Genomics
The Hospital for Sick Children
14th Floor, Toronto Medical Discovery Tower/MaRS Discovery District
101 College St., Toronto, Ontario, M5G 1L7, Canada
(416) 813-7613 (office)
(416) 813-8319 (fax)

Jenny Kaderali,
Dr. Scherer's Assistant
Phone: (416) 813-7654 x1574     Fax: (416) 813-8319

92. Crackower, M.A., Sinasac, D., Xia, J., Motoyama, J., Prochazka, M., Rommens, J.M., Scherer, S.W. and Tsui, L.-C. 1999. Cloning and characterization of two cytoplasmic dynein intermediate chain genes in mouse and human. Genomics 55, 257-267. [PMID: 10049579]
93. Minassian, B.A., Sainz, J., Serratosa, J.M., Gee, M., Sakamoto, L.M., Bohlega, S., Geoffroy, G., Barr, C., Scherer, S.W., Tomiyasu, U., Carpenter, S., Wigg, K., Sanghvi, A.V. and Delgado-Escueta, A.V. 1999. Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsy. Annals of Neurology 45, 262-265. [PMID: 9989632]
94. Tosi, S. Giudici, G., Rambaldi, A., Scherer, S.W., Bray-Ward, P., Dirscher, A., Biondi, A. and Kearney, L. 1999. Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes and comparative genomic hybridization. Genes, Chromosomes, and Cancer 24, 213-221. [PMID: 10451701]
95. Heus, H., Hing, A., van Baren, M.J., Joosse, M., Breedveld, G.J., Wang, J.C., Burgess, A., Donis-Keller, H., Berglund, C., Zguricas, J., Scherer, S.W., Rommens, J.M., Oostra, B.A. and Heutink, P. 1999. A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36. Genomics 7, 342-351. [PMID: 10329000]
96. Osborne, L.R., Campbell, T., Daradich, A., Scherer, S.W. and Tsui, L.-C. 1999. Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome. Genomics 57, 279-284. [PMID: 10198167]
97. Hwang, M-Y., Kang, Y.-J., Kim, Y-H., Scherer, S.W., Tsui, L.-C. and Sohn, U. 1999. Generation and chromosome mapping of expressed sequence tags (ESTs) from a human infant thymus. Genome 42, 457-464. [PMID: 10382293]
98. Mansour, S.J., Skaug, J., Zhao, X.-H., Giordano, J., Scherer, S.W. and Meloncon, P. 1999. p200 ARF-GEP1: A golgi-localized guanine nucleotide exchange protein whose Sec7 domain is targeted by the drug brefeldin A. Proc. Natl. Acad. Sci. U.S.A. 96, 7968-7973. [PMID: 10393931]
99. de Silva, M.G., Kantharidis, P., Scherer, S.W., Rayeroux, K., Campbell, L., Tsui, L.-C. and Zalcberg, J.R. 1999. Physical mapping of a tandem duplication on the long arm of chromosome 7 associated with a multidrug resistant phenotype. Cancer Genetics and Cytogenetics 110, 28-33. [PMID: 10198619]
100. Kobayashi, K., Sinasac, D.S., Iijima, M., Boright, A.P., Begum, L., Lee, J.R., Yasuda, T., Ikeda, S., Hirano, R., Terazono, H., Crackower, M.A., Kondo, I., Tsui, L.-C., *Scherer, S.W. and Saheki, T. 1999. The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein. Nature Genetics 22, 159-163. *corresponding author [PMID: 10369257]
101. Tosi, S., Scherer, S.W., Giudici, G., Czepulkowski, B., Biondi, A. and Kearney, L. 1999. Delineation of multiple deleted regions in 7q in myeloid disorders. Genes, Chromosomes, and Cancer 4, 384-392. [PMID: 10398433]
102. Jilani, A., Ramotar, D., Slack, C., Ong, C., Yang, X.M., Scherer, S.W. and Lasko, D.D. 1999. Molecular cloning of the human gene, PNKP, encoding a polynucleotide kinase-3'-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damage. Journal of Biological Chemistry 274, 24176-24186. [PMID: 10446192]
103. Brooks-Wilson, A., Marcil, M., Clee, S.M., Zhang, L.H., Roomp, K., van Dam, M., Yu, L., Brewer, C., Collins, J.A., Molhuizen, H.O., Loubser, O., Ouelette, B.F., Fichter, K., Ashbourne-Excoffon, K.J., Sensen, C.W., Scherer, S.W., Mott, S., Denis, M., Martindale, D., Frohlich, J., Morgan, K., Koop, B., Pimstone, S., Kastelein, J.J., Genest, J. and Hayden, M.R. 1999. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nature Genetics 22, 336-345. [PMID: 10431236]
104. Corcoran, M., Mould, S., Orchard, J., Ibbotson, R., Chapman, R., Boright, A., Platt, C., Tsui, L.-C., Scherer, S.W. and Oscier, D. 1999. Dysregulation of cyclin dependent kinase 6 expression in splenic marginal zone lymphoma through chromosome 7q translocations. Oncogene 18, 6271-6277. [PMID: 10597225]
105. Tonachini, L., Morello, R., Monticone, M., Skaug, J., Scherer, S.W., Cancedda, R. and Castagnola, P. 1999. cDNA cloning, characterization and chromosome mapping of the gene encoding human cartilage associated protein (CRTAP). Cytogenetics and Cell Genetics 87, 191-194. [PMID: 10702664]
106. Csoka, T., Scherer, S.W. and Stern, R. 1999. Expression analysis of six paralogous human hyaluronidase genes clustered on chromosome 3p21 and 7q31. Genomics 60, 356-361. [PMID: 1493834]
107. Crackower, M.A., Sinasac, D.S., Lee, J.R., Herbrick, J.-A., Tsui, L.-C. and Scherer, S.W. 1999. Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24. Cytogenetics and Cell Genetics 87, 197-198. [PMID: 10702666]
108. Sinasac, D.S., Crackower, M.A., Lee, J.R., Kobayashi, K., Saheki, T., Scherer, S.W. and Tsui, L.-C. 1999. Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13 and cloning and expression of its mouse homologue. Genomics 62, 289-292. [PMID: 10610724]
109. Leclerc, D., Odievre, M., Wu, Q., Wilson, A. Huizenga. J.J., Rozen, R., Scherer, S.W. and Gravel, R.A. 1999. Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene. Gene 240, 75-88. [PMID: 10564814]
110. Beatty, B.G., Qi, S., Pienkowska, M., Herbrick, J., Scheidl, T., Zhang, Z.M., Kola, I., Scherer, S.W. and Seth, A. 1999. Chromosomal localization of phospholipase A2 activating protein, an ETS2 target gene to 9p21. Genomics 62, 529-532. [PMID: 10644453]
111. Yousef, G.M., Luo, L.Y., Scherer, S.W., Sotiropoulou, G. and Diamandis, E.P. 1999. Molecular Characterization of Zyme/Protease M/Neurosin (PRSS9), A Hormonally Regulated Kallikrein-like Serine Protease. Genomics 62, 251-259. [PMID10610719]
112. Hadano, S., Nasir, J., Rasper, D.M., Vaillancourt, J.P., Scherer, S.W., Beatty, B.G., Ikeda, J.E., Nicholson, D.W. and Hayden, M.R. 1999. Genomic organization of the human caspase-9 gene on Chromosome 1p36.1-1p36.3. Mammalian Genome 10, 757-760. [PMID: 10384055]